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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396071Generated: November 1, 2026

Azobisisobutyronitrile → 2-Oxazolidinone, 3-acetyl-5-chloro-

https://huagongshe.com/reaction/1396071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantSulfuryl chlorideHCID 24648—
Reactant3-Acetyl-2-oxazolidinoneHCID 538766—
SolventCarbon TetrachlorideHCID 5943—
Product2-Oxazolidinone, 3-acetyl-5-chloro-HCID 12289576—

Reaction Conditions

Temperature70 °C

Reaction Steps

5.00 g of 3-acetyloxazolidin-2-one were initially charged in 25 ml of carbon tetrachloride and heated to 70° C. under an argon atmosphere. Then, alternately, a solution of 3.46 ml of sulfuryl chloride in 5 ml of carbon tetrachloride and 0.10 g of 2,2′-azobis(2-methylpropionitrile) were added, and then the mixture was stirred at the same temperature for 2 hours. After cooling to room temperature, the clear solution was decanted off from the solid residues, and the solvent was removed under reduced pressure. This gave the product (6.80 g) with a molecular weight of 163.6 g/mol (C5H6ClNO3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901114B2
Source datasetuspto-grants-2014_12
ORD IDord-a4b3da96da004f8a8730862dbe3bce08
Source noteuspto-grants-2014_12